Clinical course of sly syndrome (mucopolysaccharidosis type VII) von Montaño, Adriana M, Lock-Hock, Ngu, Steiner, Robert D, Graham, Brett H, Szlago, Marina, Greenstein, Robert, Pineda, Mercedes, Gonzalez-Meneses, Antonio, Çoker, Mahmut, Bartholomew, Dennis, Sands, Mark S, Wang, Raymond, Giugliani, Roberto, Macaya, Alfons, Pastores, Gregory, Ketko, Anastasia K, Ezgü, Fatih, Tanaka, Akemi, Arash, Laila, Beck, Michael, Falk, Rena E, Bhattacharya, Kaustuv, Franco, José, White, Klane K, Mitchell, Grant A, Cimbalistiene, Loreta, Holtz, Max, Sly, William S

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Fabry disease: the importance of the enzyme replacement therapy (TRE), treating quickly and efficiently von Juan Manuel Politei, Andrea B. Schenone, Norberto Antongiovanni, Ana María Cusumano, Gustavo Cabrera, Marina Szlago

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Initial management of acute hyperammonemia in pediatrics von Eiroa, Hernán, Durand, Consuelo, Szlago, Marina, Pereyra, Marcela, Nuñez, Mariana, Guelbert, Norberto, Pacheco, Gabriela, Kleppe, Soledad

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Fabry disease and ERT experience in 12 classic patients: Different formulations, different outcomes? von Politei, Juan, Schenone, Andrea Beatriz, Cabrera, Gustavo, Szlago, Marina

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Fabry disease and enzyme replacement therapy: 10years of experience with agalsidase beta von Politei, Juan, Schenone, Andrea, Cabrera, Gustavo, Amartino, Hernan, Szlago, Marina

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Fabry disease and enzyme replacement therapy: 10 years of experience with agalsidase beta von Politei, Juan, Schenone, Andrea, Cabrera, Gustavo, Amartino, Hernan, Szlago, Marina

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Spectrum of MOG Autoantibody-Associated Inflammatory Diseases in Pediatric Patients (I4-3A) von Tenembaum, Silvia, Waters, Patrick, Leite, Maria, Woodhall, Mark, Princich, Juan, Segura, Martin, Talarico, Maria, Szlago, Marina, Vincent, Angela

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Spectrum of MOG Autoantibody-Associated Inflammatory Diseases in Pediatric Patients (P5.275) von Tenembaum, Silvia, Waters, Patrick, Leite, Maria, Woodhall, Mark, Princich, Juan, Segura, Martin, Talarico, Maria, Szlago, Marina, Vincent, Angela

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Homovanillic acid in cerebrospinal fluid of 1388 children with neurological disorders von Molero‐Luis, Marta, Serrano, Mercedes, Ormazábal, Aida, Pérez‐Dueñas, Belén, García‐Cazorla, Àngels, Pons, Roser, Artuch, Rafael, Amartino, Hernan, Arrabal, Luisa, Campistol, Jaume, Casado, Mercedes, Castro, Pedro Castro, Cormand, Bru, Dinopoulos, Argirios, Domingo, Rosario, Duarte, Sofia T, Fernández‐Álvarez, Emilio, Desviat, Lourdes R, Hegde, Anaita, López‐Laso, Eduardo, Montero, Raquel, Ortez, Carlos, Pérez, Belén, Pineda, Mercé, Sierra, Cristina, Szlago, Marina, Schenone, Andrea B., Ruiz, Ángeles, Sequeira, Sílvia, Tondo, Mireia, Yapici, Zuhal, Iniesta, Raquel

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Erratum to: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America von Urreizti, Roser, Asteggiano, Carla, Bermudez, Marta, Córdoba, Alfonso, Szlago, Marina, Grosso, Carola, de Kremer, Raquel Dodelson, Vilarinho, Laura, D'Almeida, Vania, Martínez-Pardo, Mercedes, Peña-Quintana, Luís, Dalmau, Jaime, Bernal, Jaime, Briceño, Ignacio, Couce, María Luz, Rodés, Marga, Vilaseca, Maria Antonia, Balcells, Susana, Grinberg, Daniel

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Molecular characterization of 22 novel UDP-N-acetylglucosamine-1-phosphate transferase α- and β-subunit (GNPTAB) gene mutations causing mucolipidosis types IIα/β and IIIα/β in 46 p... von Tappino, Barbara, Chuzhanova, Nadia A, Regis, Stefano, Dardis, Andrea, Corsolini, Fabio, Stroppiano, Marina, Tonoli, Emmanuel, Beccari, Tommaso, Rosano, Camillo, Mucha, Jan, Blanco, Mariana, Szlago, Marina, Di Rocco, Maja, Cooper, David N, Filocamo, Mirella

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Molecular analysis of HEXA gene in Argentinean patients affected with Tay–Sachs disease: Possible common origin of the prevalent c.459+5A>G mutation von Zampieri, Stefania, Montalvo, Annalisa, Blanco, Mariana, Zanin, Irene, Amartino, Hernan, Vlahovicek, Kristian, Szlago, Marina, Schenone, Andrea, Pittis, Gabriela, Bembi, Bruno, Dardis, Andrea

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Manejo inicial de la hiperamonemia aguda en pediatría von Eiroa, Hernán, Durand, Consuelo, Szlago, Marina, Pereyra, Marcela, Nuñez, Mariana, Guelbert, Norberto, Pacheco, Gabriela, Kleppe, Soledad

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Osteoporosis-pseudoglioma Syndrome: a pediatric case of primary osteoporosis von Braslavsky, Debora, Scaglia, Paula, Sanguineti, Nora, Aza-Carmona, Miriam, Blanco, Julian Nevado, Lapunzina Badia, Pablo D., Fernandez, Maria del C., Ruiz, Olivia, Carmona, Alejandra, Szlago, Marina, Arberas, Claudia, Cassinelli, Hamilton, Heath, Karen, Rey, Rodolfo, Bergada, Ignacio

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Morquio disease (Mucopolysaccharidosis type IV-A): clinical aspects, diagnosis and new treatment with enzyme replacement therapy von Politei, Juan, Schenone, Andrea B, Guelbert, Norberto, Fainboim, Alejandro, Szlago, Marina

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Mucopolysaccharidosis type VI: clinical aspects, diagnosis and treatment with enzyme replacement therapy von Politei, Juan, Schenone, Andrea, Blanco, Mariana, Szlago, Marina

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121. Assessment and biochemical diagnosis of MPS IV in Argentina von Schenone, Andrea B., Szlago, Marina, Gagioli, Daniela, Blanco, Mariana

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Mucopolysaccharidosis VI: Evaluation After 2 Years of Treatment von Politei, Juan, Schenone, Andrea Beatriz, Gustavo, Cabrera, Alejandra, Antacle, Marina, Szlago

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Myoclonus and angiokeratomas in adult galactosialidosis von Abaroa, Luz, Garretto, Nelida S., Arakaki, Tomoko, Kauffman, Marcelo, Moron, Dolores G., Figueredo, Alex M., Szlago, Marina, Metman, Leo Verhagen

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Acetyl-L-Carnitine and Nicotinamide for Prevention of Type 1 Diabetes. I-Literature Review which Gave Support to the Treatment. II-Case Report, Evaluation of Five Years Treatment von Miriam Tonietti, Ivana Fernandez

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